Wikipedia

Hexachlorobenzene

Hexachlorobenzene, or perchlorobenzene, is an aryl chloride and a six-substituted chlorobenzene with the molecular formula C6Cl6. It is a fungicide formerly used as a seed treatment, especially on wheat to control the fungal disease bunt. It has been banned globally under the Stockholm Convention on Persistent Organic Pollutants.[6]

Hexachlorobenzene
Skeletal formula of hexachlorobenzene
Skeletal formula of hexachlorobenzene
Ball-and-stick model of hexachlorobenzene
Ball-and-stick model of hexachlorobenzene
Names
Preferred IUPAC name
Hexachlorobenzene
Other names
Perchlorobenzene; HCB; Julin's chloride of carbon
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.886 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9 checkY
    Key: CKAPSXZOOQJIBF-UHFFFAOYSA-N checkY
  • InChI=1/C6Cl6/c7-1-2(8)4(10)6(12)5(11)3(1)9
    Key: CKAPSXZOOQJIBF-UHFFFAOYAV
  • c1(Cl)c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
Properties
C6Cl6
Molar mass 284.77 g·mol−1
Appearance White crystalline solid
Density 2.04 g/cm3
Melting point 228.83 °C (443.89 °F; 501.98 K)[1]
Boiling point 325 °C (617 °F; 598 K)[1]
insoluble
Solubility in other solvents slightly soluble in ethanol; soluble in diethyl ether and chloroform; very soluble in benzene[1]
log P 5.47[2]
−147.0·10−6 cm3/mol[3]
Thermochemistry[5]
201.2 J·mol−1·K−1
260.2 J·mol−1·K−1
−127.6 kJ·mol−1
Enthalpy of fusion (ΔfH⦵fus)
 25.2 kJ·mol−1[4]
Related compounds
Related compounds
 Benzene
Hexafluorobenzene
Hexabromobenzene
Hexaiodobenzene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Physical and chemical properties

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Hexachlorobenzene is a stable, white, crystalline chlorinated hydrocarbon.[7] It is sparingly soluble in organic solvents such as benzene, diethyl ether and alcohol, but practically insoluble in water with no reaction. It has a flash point of 468 °F and it is stable under normal temperatures and pressures. It is combustible but it does not ignite readily. When heated to decomposition, hexachlorobenzene emits highly toxic fumes of hydrochloric acid, other chlorinated compounds (such as phosgene), carbon monoxide, and carbon dioxide.[8]

History

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Hexachlorobenzene was first known as "Julin's chloride of carbon" as it was discovered as a strange and unexpected product of impurities reacting in Julin's nitric acid factory.[9] In 1864, Hugo Müller synthesised the compound by the reaction of benzene and antimony pentachloride, he then suggested that his compound was the same as Julin's chloride of carbon.[10] Müller previously also believed it was the same compound as Michael Faraday's "perchloride of carbon" (Hexachloroethane), obtained a small sample of Julin's chloride of carbon to send to Richard Phillips and Faraday for investigation.[9] In 1867, Henry Bassett proved that the compound produced from benzene and antimony was the same as Julian's carbon chloride and named it "hexachlorobenzene".[10][9]

Leopold Gmelin named it "dichloride of carbon" and claimed that the carbon was derived from cast iron and the chlorine was from crude saltpetre.[9]

Victor Regnault obtained hexachlorobenzene from the decomposition of chloroform and tetrachloroethylene vapours through a red-hot tube.[9]

Synthesis

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Large-scale manufacture for use as a fungicide was developed by using the residue remaining after purification of the mixture of isomers of hexachlorocyclohexane, from which the insecticide lindane (the γ-isomer) had been removed, leaving the unwanted α- and β- isomers. This mixture is produced when benzene is reacted with chlorine in the presence of ultraviolet light (e.g. from sunlight).[11][12] However, manufacture is no longer practiced following the compound's ban.

Hexachlorobenzene has been made on a laboratory scale since the 1890s, by the electrophilic aromatic substitution reaction of chlorine with benzene or chlorobenzenes.[13] A typical catalyst is ferric chloride. Much milder reagents than chlorine (e.g. dichlorine monoxide, iodine in chlorosulfonic acid) also suffice, and the various hexachlorocyclohexanes can substitute for benzene as well.[14]

Usage

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Hexachlorobenzene was used in agriculture to control the fungus tilletia caries (common bunt of wheat). It is also effective on tilletia controversa, dwarf bunt. The compound was introduced in 1947, normally formulated as a seed dressing but is now banned in many countries.[15]

A minor industrial phloroglucinol synthesis nucleophilically substitutes hexachlorobenzene with alkoxides, followed by acidic workup.[16]

Safety

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Hexachlorobenzene can react violently with dimethylformamide, particularly in the presence of catalytic transition-metal salts.[17]

Toxicology

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  • Oral LD50 (rat): 10,000 mg/kg
  • Oral LD50 (mice): 4,000 mg/kg
  • Inhalation LC50 (rat): 3600 mg/m3

Material has relatively low acute toxicity but is toxic because of its persistent and cumulative nature in body tissues in rich lipid content.[citation needed]

Hexachlorobenzene is an animal carcinogen and is considered to be a probable human carcinogen.[18] After its introduction as a fungicide in 1945, for crop seeds, this toxic chemical was found in all food types.[citation needed] Hexachlorobenzene was banned from use in the United States in 1966.

This material has been classified by the International Agency for Research on Cancer (IARC) as a Group 2B carcinogen (possibly carcinogenic to humans). Animal carcinogenicity data for hexachlorobenzene show increased incidences of liver, kidney (renal tubular tumours) and thyroid cancers.[19] Chronic oral exposure in humans has been shown to give rise to a liver disease (porphyria cutanea tarda), skin lesions with discoloration, ulceration, photosensitivity, thyroid effects, bone effects and loss of hair. Neurological changes have been reported in rodents exposed to hexachlorobenzene. Hexachlorobenzene may cause embryolethality and teratogenic effects. Human and animal studies have demonstrated that hexachlorobenzene crosses the placenta to accumulate in foetal tissues and is transferred in breast milk.

HCB is very toxic to aquatic organisms. It may cause long term adverse effects in the aquatic environment. Therefore, release into waterways should be avoided. It is persistent in the environment. Ecological investigations have found that biomagnification up the food chain does occur. Hexachlorobenzene has a half life in the soil of between 3 and 6 years. Risk of bioaccumulation in an aquatic species is high.

Anatolian porphyria

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In Anatolia, Turkey between 1955 and 1959, during a period when bread wheat was unavailable, 500 people were fatally poisoned and more than 4,000 people fell ill by eating bread made with HCB-treated seed that was intended for agriculture use. Most of the sick were affected with a liver condition called porphyria cutanea tarda, which disturbs the metabolism of hemoglobin and results in skin lesions. Almost all breastfeeding children under the age of two, whose mothers had eaten tainted bread, died from a condition called "pembe yara" or "pink sore", most likely from high doses of HCB in the breast milk.[20] In one mother's breast milk the HCB level was found to be 20 parts per million in lipid, approximately 2,000 times the average levels of contamination found in breast-milk samples around the world.[21][22] Follow-up studies 20 to 30 years after the poisoning found average HCB levels in breast milk were still more than seven times the average for unexposed women in that part of the world (56 specimens of human milk obtained from mothers with porphyria, average value was 0.51 ppm in HCB-exposed patients compared to 0.07 ppm in unexposed controls),[23][24] and 150 times the level allowed in cow's milk.[25]

In the same follow-up study of 252 patients (162 males and 90 females, avg. current age of 35.7 years), 20–30 years' postexposure, many subjects had dermatologic, neurologic, and orthopedic symptoms and signs. The observed clinical findings include scarring of the face and hands (83.7%), hyperpigmentation (65%), hypertrichosis (44.8%), pinched faces (40.1%), painless arthritis (70.2%), small hands (66.6%), sensory shading (60.6%), myotonia (37.9%), cogwheeling (41.9%), enlarged thyroid (34.9%), and enlarged liver (4.8%). Urine and stool porphyrin levels were determined in all patients, and 17 have at least one of the porphyrins elevated. Offspring of mothers with three decades of HCB-induced porphyria appear normal.[23]

See also

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References

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Cited works

  1. ^ a b c Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. p. 3-276. ISBN 978-1-4200-9084-0.
  2. ^ Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. p. 16-42. ISBN 978-1-4200-9084-0.
  3. ^ Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. p. 3-674. ISBN 978-1-4200-9084-0.
  4. ^ Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. p. 6-137. ISBN 978-1-4200-9084-0.
  5. ^ Lide, David R., ed. (2009). CRC Handbook of Chemistry and Physics (90th ed.). Boca Raton, Florida: CRC Press. p. 5-30. ISBN 978-1-4200-9084-0.
  6. ^ Stockholm Convention on Persistent Organic Pollutants website Archived 2014-04-16 at the Wayback Machine
  7. ^ PubChem. "Hexachlorobenzene". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-03-24.
  8. ^ "RoC Profile: Hezachlorobenzene" (PDF). National Toxicology Program.
  9. ^ a b c d e Roscoe, H. E., Schorlemmer, C. (1887). The chemistry of the hydrocarbons and their derivatives, or Organic chemistry. 1882-1892. 6 v. USA: D. Appleton. Pages 83-83
  10. ^ a b On Julin's Chloride of Carbon, Henry Bassett, J. Chem. Soc., 1867,20, 443-444 [1]
  11. ^ US patent 2773104, Ligett, Waldo B., "Manufacture of hexachlorobenzene", issued 1956-12-04, assigned to Ethyl Corp 
  12. ^ US patent 2792434, Becke, Friedrich & Sperber, Heinrich, "Process for the production of hexachlorobenzene", issued 1957-05-14, assigned to BASF 
  13. ^ Cohen, Julius Berend; Hartley, Percival (1905). "CXXXV.—Studies in chlorination. III. The progressive chlorination of benzene in presence of the aluminium-mercury couple". J. Chem. Soc., Trans. 87: 1360–1367. doi:10.1039/CT9058701360.
  14. ^ Beck, Uwe; Löser, Eckhard (2012). "Chlorinated benzenes and other nucleus-chlorinated aromatic hydrocarbons". Ullmann's Encyclopedia of Industrial Chemistry. Vol. 8. Weinheim: Wiley-VCH. p. 494. doi:10.1002/14356007.o06_o03. ISBN 978-3527306732.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link)
  15. ^ Pesticide Properties Database. "Hexachlorobenzene". University of Hertfordshire. Retrieved 2022-06-13.
  16. ^ Fiege, Helmut; Voges, Heinz-Werner; Hamamoto Toshikazu; Umemura Sumio; Iwata Tadao; Miki Hisaya; Fujita Yasuhiro; Buysch, Hans-Joseph; Garbe, Dorothea; Paulus, Wilfried (2012). "Phenol derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Vol. 26. Weinheim: Wiley-VCH. p. 558. doi:10.1002/14356007.a19_313. ISBN 978-3527306732.
  17. ^ Marsella, John A.; et al., "Dimethylformamide", Kirk-Othmer Encyclopedia of Chemical Technology, New York: John Wiley, p. 6, doi:10.1002/0471238961.0409130513011819.a01.pub2, ISBN 9780471238966
  18. ^ "Report on Carcinogens, Eleventh Edition" (PDF). Archived (PDF) from the original on 2009-11-14. (208 KB)
  19. ^ "Hexachlorobenzene". The Carcinogenic Potency Database Project. Retrieved 2020-06-07.
  20. ^ Natural Resources Defense Council (2001). Healthy Milk, Healthy Baby: Chemical Pollution and Mother's Milk. Retrieved September 13, 2008 from the World Wide Web: http://www.nrdc.org/breastmilk/chem4.asp
  21. ^ Jensen, A.A. and S.A. Slorach. Chemical Contaminants in Human Milk, 1991, Boca Raton Ann Arbor Boston: CRC Press, Inc.
  22. ^ Courtney, K.D. Hexachlorobenzene (HCB): A Review, Environmental Research 1979; 20: p. 225-266.
  23. ^ a b Gocmen, A., et al. Hexachlorobenzene Episode in Turkey, Biomedical Environmental Science 1989; 2(1): p. 36-43.
  24. ^ Cripps, D.J., et al. Porphyria Turcica Due to Hexachlorobenzene: A 20 to 30 Year Follow-up Study on 204 Patients, British Journal of Dermatology 1984; 111(4): p. 413-422.
  25. ^ Peters, H.A., et al. Epidemiology of Hexachlorobenzene-induced Porphyria in Turkey: Clinical and Laboratory Follow-up After 25 Years, Archives of Neurology 1982; 39(12): p. 744-749.

Additional references

  • International Agency for Research on Cancer. In: IARC Monographs on the Evaluation of Carcinogenic Risk to Humans. World Health Organisation, Vol 79, 2001pp 493–567
  • Registry of Toxic Effects of Chemical Substances. Ed. D. Sweet, US Dept. of Health & Human Services: Cincinnati, 2005.
  • Environmental Health Criteria No 195; International Programme on Chemical Safety, World health Organization, Geneva, 1997.
  • Toxicological Profile for Hexachlorobenzene (Update), US Dept of Health & Human Services, Sept 2002.
  • Merck Index, 11th Edition, 4600
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